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illumina iscan microarray scanner  (Illumina Inc)


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    Structured Review

    Illumina Inc illumina iscan microarray scanner
    Pedigree and genetic analysis for family 1. (A) Genetic pedigree of family 1; black circle II.1 indicates the affected child (P1). (B) SeqPilot ® CNV analysis: reduced copy number for the RUNX1 exons for the index patient (green columns) compared to the patients analyzed in the same enrichment (blue), indicating a heterozygous RUNX1 -gene deletion. (C) Chromosomal <t>microarray</t> analysis: 1.56 Mb deletion (21q22.11q22.12 shown as a red bar) including RUNX1 .
    Illumina Iscan Microarray Scanner, supplied by Illumina Inc, used in various techniques. Bioz Stars score: 97/100, based on 1618 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/iscan+microarray+scanner/pmc12739554-93-8-8?v=Illumina+Inc
    Average 97 stars, based on 1618 article reviews
    illumina iscan microarray scanner - by Bioz Stars, 2026-07
    97/100 stars

    Images

    1) Product Images from "RUNX1-FPDMM in families with mild thrombocytopenia and platelet function anomalies: a case series"

    Article Title: RUNX1-FPDMM in families with mild thrombocytopenia and platelet function anomalies: a case series

    Journal: Frontiers in Medicine

    doi: 10.3389/fmed.2025.1657054

    Pedigree and genetic analysis for family 1. (A) Genetic pedigree of family 1; black circle II.1 indicates the affected child (P1). (B) SeqPilot ® CNV analysis: reduced copy number for the RUNX1 exons for the index patient (green columns) compared to the patients analyzed in the same enrichment (blue), indicating a heterozygous RUNX1 -gene deletion. (C) Chromosomal microarray analysis: 1.56 Mb deletion (21q22.11q22.12 shown as a red bar) including RUNX1 .
    Figure Legend Snippet: Pedigree and genetic analysis for family 1. (A) Genetic pedigree of family 1; black circle II.1 indicates the affected child (P1). (B) SeqPilot ® CNV analysis: reduced copy number for the RUNX1 exons for the index patient (green columns) compared to the patients analyzed in the same enrichment (blue), indicating a heterozygous RUNX1 -gene deletion. (C) Chromosomal microarray analysis: 1.56 Mb deletion (21q22.11q22.12 shown as a red bar) including RUNX1 .

    Techniques Used: Microarray



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    Pedigree and genetic analysis for family 1. (A) Genetic pedigree of family 1; black circle II.1 indicates the affected child (P1). (B) SeqPilot ® CNV analysis: reduced copy number for the RUNX1 exons for the index patient (green columns) compared to the patients analyzed in the same enrichment (blue), indicating a heterozygous RUNX1 -gene deletion. (C) Chromosomal <t>microarray</t> analysis: 1.56 Mb deletion (21q22.11q22.12 shown as a red bar) including RUNX1 .
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    Image Search Results


    Pedigree and genetic analysis for family 1. (A) Genetic pedigree of family 1; black circle II.1 indicates the affected child (P1). (B) SeqPilot ® CNV analysis: reduced copy number for the RUNX1 exons for the index patient (green columns) compared to the patients analyzed in the same enrichment (blue), indicating a heterozygous RUNX1 -gene deletion. (C) Chromosomal microarray analysis: 1.56 Mb deletion (21q22.11q22.12 shown as a red bar) including RUNX1 .

    Journal: Frontiers in Medicine

    Article Title: RUNX1-FPDMM in families with mild thrombocytopenia and platelet function anomalies: a case series

    doi: 10.3389/fmed.2025.1657054

    Figure Lengend Snippet: Pedigree and genetic analysis for family 1. (A) Genetic pedigree of family 1; black circle II.1 indicates the affected child (P1). (B) SeqPilot ® CNV analysis: reduced copy number for the RUNX1 exons for the index patient (green columns) compared to the patients analyzed in the same enrichment (blue), indicating a heterozygous RUNX1 -gene deletion. (C) Chromosomal microarray analysis: 1.56 Mb deletion (21q22.11q22.12 shown as a red bar) including RUNX1 .

    Article Snippet: Scanning and image acquisition were performed using an Illumina iScan microarray scanner.

    Techniques: Microarray